Anemia due to membrane defect
Autosomal hereditary disorder
Erythrocyte membrane abnormality
Hereditary hemolytic anemia
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Hereditary spherocytosis (disorder)
Hereditary spherocytosis
HS - Hereditary spherocytosis
Minkowsky-Chauffard syndrome
Familial spherocytosis
Congenital spherocytic hemolytic anemia
Congenital spherocytosis
Familial acholuric jaundice
hereditaire sferocytose
Id55995005
StatusPrimitive
Associated morphologySpherocyte
Finding siteErythrocyte
Has interpretationBelow reference range
InterpretsRed blood cell count
Has interpretationBelow reference range
InterpretsMeasurement of total hemoglobin concentration
Has interpretationPresent
InterpretsHemolysis
PALGA thesaurus simple reference set for pathology
General Practice / Family Practice reference set
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetD58.0
RuleTRUE
AdviceALWAYS D58.0
CorrelationSNOMED CT source code to target map code correlation not specified
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Hereditary spherocytosis due to beta spectrin defect
Hereditary spherocytosis due to deficiency of protein 4.2
Hereditary spherocytosis due to spectrin deficiency3